Evidence map›Paper›PMID 42434841›Full record

ArticleAdvanced healthcare materials2026

Carrier-Free Nanoparticles Enhance Photothermal-Immune Therapy via Metabolic Reprogramming in Triple-Negative Breast Cancer.

Yanxian Hou, Yingfeng Cheng, Yinhao Lin, Huixiang Sheng, Xiaoyan Mao, Zhounan Li, Zhanzheng Ye, Linying Wang, Yongshuai Kang, Jinyao Ye and 4 more

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Yanxian HouWenzhou Municipal Key Laboratory of Pediatric Pharmacy, Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Yingfeng ChengWenzhou Municipal Key Laboratory of Pediatric Pharmacy, Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Yinhao LinWenzhou Municipal Key Laboratory of Pediatric Pharmacy, Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Huixiang ShengWenzhou Municipal Key Laboratory of Pediatric Pharmacy, Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Xiaoyan MaoWenzhou Municipal Key Laboratory of Pediatric Pharmacy, Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Zhounan LiWenzhou Municipal Key Laboratory of Pediatric Pharmacy, Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Zhanzheng YeWenzhou Municipal Key Laboratory of Pediatric Pharmacy, Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Linying WangWenzhou Municipal Key Laboratory of Pediatric Pharmacy, Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Yongshuai KangWenzhou Municipal Key Laboratory of Pediatric Pharmacy, Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Jinyao YeWenzhou Municipal Key Laboratory of Pediatric Pharmacy, Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Qing YaoWenzhou Municipal Key Laboratory of Pediatric Pharmacy, Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.ORCID https://orcid.org/0000-0003-0115-9075
Longfa KouWenzhou Municipal Key Laboratory of Pediatric Pharmacy, Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.ORCID https://orcid.org/0000-0001-8502-4279
Shihui BaoWenzhou Municipal Key Laboratory of Pediatric Pharmacy, Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Ruijie ChenWenzhou Municipal Key Laboratory of Pediatric Pharmacy, Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.

Funding

Clinical Drug Evaluation and Research Special Scientific Funding Project of the Zhejiang Province Pharmaceutical Association 2025ZJLP05Natural Science Foundation of Zhejiang Province LQN25H300008
6 · The paper itself

Abstract

A carrier-free co-assembled nanoplatform, designated as IR@PF-M NPs, was developed to enhance photothermal-immunotherapy against triple-negative breast cancer (TNBC) by reprogramming methionine metabolism. The nanoplatform was constructed through the self-assembly of the methionine adenosyltransferase 2A (MAT2A) inhibitor PF9366 with the near-infrared (NIR)-absorbing dye IR808, followed by surface modification with DSPE-PEG2000-Met. This formulation exhibited dual targeting capabilities, enabling tumor accumulation via the enhanced permeability and retention effect and selective uptake by tumor cells through overexpressed methionine transporters, which together enhanced intratumoral accumulation and photothermal efficiency. Upon NIR irradiation, IR808 generated potent photothermal effects with intratumoral temperature beyond 50°C that induced immunogenic cell death (ICD) and transformed the tumor microenvironment into an immune-activated ("hot") state. Simultaneously, PF9366 disrupted methionine metabolism, further amplifying ICD and suppressing TNBC progression and metastasis. By integrating photothermal therapy with metabolic intervention, IR@PF-M NPs demonstrated superior antitumor efficacy and immunomodulatory activity, offering a promising therapeutic strategy for TNBC management.

Indexed as

ImmunotherapyNanoparticlesPhotothermal TherapyTriple Negative Breast NeoplasmsAnimalsCell Line, TumorFemaleHumansIndolesMetabolic ReprogrammingMethionineMiceMice, Inbred BALB CMice, NudeTumor Microenvironment2-(2-(2-chloro-3-((1,3-dihydro-3,3-dimethyl-1-propyl-2H-indol-2-ylidene)ethylidene)-1-cyclohexen-1-yl)ethenyl)-3,3-dimethyl-1-propylindoliumIndolesMethioninecarrier‐free co‐assemblymethionine metabolismphotothermal immunotherapytriple‐negative breast cancertumor immune microenvironment

Identifiers

PMID42434841
PMCPMC13474129

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.